Reprogramming of gastrointestinal cancer cells

被引:8
作者
Dewi, DyahLaksmi [1 ,2 ]
Ishii, Hideshi [2 ]
Haraguchi, Naotsugu [2 ]
Nishikawa, Shimpei [1 ,2 ]
Kano, Yoshihiro [1 ,2 ]
Fukusumi, Takahito [1 ,2 ]
Ohta, Katsuya [1 ,2 ]
Miyazaki, Susumu [1 ]
Ozaki, Miyuki [1 ,2 ]
Sakai, Daisuke [2 ]
Satoh, Taroh [2 ]
Nagano, Hiroaki [1 ]
Doki, Yuichiro [1 ]
Mori, Masaki [1 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Surg Gastroenterol, Osaka, Japan
[2] Osaka Univ, Grad Sch Med, Dept Frontier Sci Canc & Chemotherapy, Osaka, Japan
来源
CANCER SCIENCE | 2012年 / 103卷 / 03期
关键词
PLURIPOTENT STEM-CELLS; TUMOR-SUPPRESSOR; SOMATIC-CELLS; HUMAN FIBROBLASTS; DEFINED FACTORS; SENDAI-VIRUS; GENERATION; MOUSE; INDUCTION; MIR-302;
D O I
10.1111/j.1349-7006.2011.02184.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cell reprogramming reverts cells to multipotent, preprogrammed states by re-establishing epigenetic markers. It can also induce considerable malignant phenotype modification. Because key events in cancer relapse and metastasis, including epithelialmesenchymal transition phenotypes, are regulated primarily by reversible and transient epigenetic modifications rather than the accumulation of irreversible and stable genetic abnormalities, studying dynamic mechanisms regulating these biological processes is important. Transcription factors for induced pluripotent stem cells and non-coding microRNAs allow pluripotent phenotype induction. We present the current knowledge of the possible applications of cell reprogramming in reducing aggressive phenotype expression, which can induce tumor cell hibernation and maintain appropriate phenotypes, thereby minimizing relapse and metastasis after surgical resection of gastrointestinal cancer. (Cancer Sci 2012; 103: 393399)
引用
收藏
页码:393 / 399
页数:7
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